IFITM proteins: Understanding their diverse roles in viral infection, cancer, and immunity.

J Biol Chem

Infection Medicine, School of Biomedical Sciences, University of Edinburgh, Edinburgh, United Kingdom; ZJU-UoE Institute, Zhejiang University, Haining, Zhejiang, China. Electronic address:

Published: January 2023

AI Article Synopsis

  • Interferon-induced transmembrane proteins (IFITMs) are key antiviral agents that block the entry of various important viruses like influenza A, HIV-1, and Dengue by disrupting the fusion of viral and cell membranes.
  • Recent research has revealed that IFITMs also provide mechanisms to restrict viruses after they have entered the cell and play roles in regulating both innate and adaptive immune responses.
  • Additionally, IFITMs may be connected to cancer progression, as their expression might indicate more aggressive forms of the disease and resistance to treatment, prompting investigations into their diverse functions for a better understanding of IFITM biology.

Article Abstract

Interferon-induced transmembrane proteins (IFITMs) are broad spectrum antiviral factors that inhibit the entry of a wide range of clinically important pathogens including influenza A virus, HIV-1, and Dengue virus. IFITMs are thought to act primarily by antagonizing virus-cell membrane fusion in this regard. However, recent work on these proteins has uncovered novel post-entry viral restriction mechanisms. IFITMs are also increasingly thought to have a role regulating immune responses, including innate antiviral and inflammatory responses as well as adaptive T-cell and B-cell responses. Further, IFITMs may have pathological activities in cancer, wherein IFITM expression can be a marker of therapeutically resistant and aggressive disease courses. In this review, we summarize the respective literatures concerning these apparently diverse functions with a view to identifying common themes and potentially yielding a more unified understanding of IFITM biology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800550PMC
http://dx.doi.org/10.1016/j.jbc.2022.102741DOI Listing

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